Vemuri R, Haberland M E, Fong D, Philipson K D
Department of Physiology, University of California, Los Angeles.
J Membr Biol. 1990 Dec;118(3):279-83. doi: 10.1007/BF01868612.
We have previously partially purified the sarcolemmal Na(+)-Ca2+ exchange protein and produced rabbit polyclonal antibodies to the exchanger (Philipson, K.D., Longoni, S., Ward, R. 1988. Biochim. Biophys. Acta 945:298-306). We now describe the generation of three stable murine hybridoma lines which secrete monoclonal antibodies (MAb's) to the exchanger. These MAb's immunoprecipitate 50-75% of solubilized Na(+)-Ca2+ exchange activity. The MAb's appear to be reactive with native conformation-dependent epitopes on the Na(+)-Ca2+ exchanger since they do not react on immunoblots. An indirect method was used to identify Na(+)-Ca2+ exchange proteins. A column containing Na(+)-Ca2+ exchanger immobilized by MAb's was used to affinity purify the rabbit polyclonal antibody. The affinity-purified polyclonal antibody reacted with proteins of apparent molecular weights of 70, 120, and 160 kDa on immunoblots of sarcolemma. The data provide strong support for our previous association of Na(+)-Ca2+ exchange with these proteins.
我们之前已对肌膜钠钙交换蛋白进行了部分纯化,并制备了针对该交换蛋白的兔多克隆抗体(菲利普森,K.D.,隆戈尼,S.,沃德,R. 1988年。《生物化学与生物物理学报》945:298 - 306)。我们现在描述三种稳定的小鼠杂交瘤细胞系的产生,这些细胞系分泌针对该交换蛋白的单克隆抗体(MAb)。这些MAb可免疫沉淀50 - 75%的可溶钠钙交换活性。这些MAb似乎与钠钙交换蛋白上依赖天然构象的表位发生反应,因为它们在免疫印迹上不发生反应。采用间接方法鉴定钠钙交换蛋白。使用一个含有通过MAb固定的钠钙交换蛋白的柱子来亲和纯化兔多克隆抗体。亲和纯化的多克隆抗体在肌膜免疫印迹上与表观分子量为70、120和160 kDa的蛋白质发生反应。这些数据为我们之前关于钠钙交换与这些蛋白质的关联提供了有力支持。